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Otx2 Binding to Perineuronal Nets Persistently Regulates Plasticity in the Mature Visual Cortex
Open accessAbstract
Specific transfer of (orthodenticle homeobox 2) Otx2 homeoprotein into GABAergic interneurons expressing parvalbumin (PV) is necessary and sufficient to open, then close, a critical period (CP) of plasticity in the developing mouse visual cortex. The accumulation of endogenous Otx2 in PV cells suggests the presence of specific Otx2 binding sites. Here, we find that perineuronal nets (PNNs) on the surfaces of PV cells permit the specific, constitutive capture of Otx2. We identify a 15 aa domain containing an arginine-lysine doublet (RK peptide) within Otx2, bearing prototypic traits of a glycosaminoglycan (GAG) binding sequence that mediates Otx2 binding to PNNs, and specifically to chondroitin sulfate D and E, with high affinity. Accordingly, PNN hydrolysis by chondroitinase ABC reduces the amount of endogenous Otx2 in PV cells. Direct infusion of RK peptide similarly disrupts endogenous Otx2 localization to PV cells, reduces PV and PNN expression, and reopens plasticity in adult mice. The closure of one eye during this transient window reduces cortical acuity and is specific to the RK motif, as an Alanine-Alanine variant or a scrambled peptide fails to reactivate plasticity. Conversely, this transient reopening of plasticity in the adult restores binocular vision in amblyopic mice. Thus, one function of PNNs is to facilitate the persistent internalization of Otx2 by PV cells to maintain CP closure. The pharmacological use of the Otx2 GAG binding domain offers a novel, potent therapeutic tool with which to restore cortical plasticity in the mature brain.
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In the citing paper
“Across multiple neuropsychiatric disorders, including autism, schizophrenia, and bipolar disorder, the developmental gene expression program in PV cells is instead immature (54).”
From Perineuronal nets protect fast-spiking interneurons against oxidative stress (2013) · cites this paper as [54]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“While OTX2 and Sema3A bind to 4,6 disulphated GAGs in the PNNs [23, 28], Nptx2 binds to both 4,6 sulphated GAGs and HA [29].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [23]
The cited source says what the claim attributes to it.
In the citing paper
“The soluble transcription factor OTX2 binds to PNNs and is internalised, leading to maturation of PV neurons and maintenance of PNNs in adulthood [23, 26].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [23]
The cited source says what the claim attributes to it.
In the citing paper
“Otx--2, which maintains PNNs (Beurdeley et al., 2012;Bernard and Prochiantz, 2016)”
From Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity (2016) · cites this paper as Beurdeley et al., 2012
In the citing paper
“Compromised PNNs prevent the persistent uptake of Otx2 homeoprotein into the enwrapped PV-cells needed for their maturation (including PNN maintenance itself) (27, 40, 41).”
From Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons (2015) · cites this paper as [41]
In the citing paper
“Subsequent inability to engage downstream molecular pathways by Otx2 within the PV-cell would retain a juvenile plastic state (41).”
From Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons (2015) · cites this paper as [41]
In the citing paper
“Second, PNN disruption prevents the persistent uptake of Otx2 homeoprotein into the enwrapped PV-cells required for their maintenance (27, 40, 41) (Fig. S3).”
From Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons (2015) · cites this paper as [41]
In the citing paper
“This may offer novel strategies or drug targets, in addition to antioxidants (18, 25) or Otx2 up-regulation (41, 51), for correcting aberrant brain plasticity in mental illness.”
From Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons (2015) · cites this paper as [41]
In the citing paper
“Importantly, the second threshold is ‘reversible’ as decreasing Otx2 concentration engages the plastic regime (this study; (Beurdeley et al., 2012)).”
From Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity (2013) · cites this paper as Beurdeley et al., 2012
In the citing paper
“The model also stipulates that early sensory experience (sensory input) initiates expression of Otx2 binding sites on nascent PNNs (Beurdeley et al., 2012; Miyata et al., 2012), facilitating Otx2 import and opening a period of plasticity.”
From Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity (2013) · cites this paper as Beurdeley et al., 2012
In the citing paper
“The same scheme also explain show a general source, thanks to mature, fully assembled PNNs, participates in maintaining a non-plastic state, allowing for the possibility to reopen plasticity in adulthood (Beurdeley et al., 2012; Pizzorusso et al., 2002).”
From Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity (2013) · cites this paper as Beurdeley et al., 2012
In the citing paper
“and that the permanent transfer of Otx2 through PNN recognition is necessary to repress plasticity in the adult (Beurdeley et al., 2012).”
From Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity (2013) · cites this paper as Beurdeley et al., 2012
In the citing paper
“Once formed, and throughout adulthood, PNNs control neuronal access to growth and transcription factors, stabilize synaptic connectivity and compartmentalize the neuronal surface, regulating the availability of glutamatergic receptors to postsynaptic specializations and, thus, neuronal firing properties.23, 25, 38”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [38]
In the citing paper
“Interestingly, PNNs have been proposed as indispensable mediators of the modulation of synaptic plasticity by the transcription factor Otx259–61.”
From Elimination of the four extracellular matrix molecules tenascin-C, tenascin-R, brevican and neurocan alters the ratio of excitatory and inhibitory synapses (2019) · cites this paper as [59]
In the citing paper
“In fact, PV and PNN colocalization is correlated with critical period closure and reduced synaptic plasticity, particularly in sensory cortices (Nowicka et al., 2009; Beurdeley et al., 2012).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Beurdeley et al., 2012
In the citing paper
“PNNs are necessary for the uptake of Otx2 by PV cells, which promotes PV cell maturation (Beurdeley et al., 2012).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Beurdeley et al., 2012
In the citing paper
“Studies of rodent visual cortex development indicate that Otx2 is localized to GABAergic cells, and is more likely found in PV cells that are enwrapped with PNNs, which contain a specific Otx2 binding site (Beurdeley et al., 2012).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Beurdeley et al., 2012
In the citing paper
“Long believed to be responsible primarily for structural support, PNNs have in recent years come to the forefront of neuroscience research as critical elements regulating synaptic functions and plasticity during development and adulthood (Beurdeley et al., 2012; Dityatev et al., 2010; Gogolla et al., 2009; Gundelfinger et al., 2010; Pizzorusso et al., 2002; Xue et al., 2014; Yamada and Jinno, 2013”
From Losing the sugar coating: Potential impact of perineuronal net abnormalities on interneurons in schizophrenia (2015) · cites this paper as Beurdeley et al., 2012
In the citing paper
“this homeoprotein signals the maturation of the parvalbumin-containing GABAergic interneurons, which contributes to the opening and possibly also the closure of the critical period”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Beurdeley et al., 2012
In the citing paper
“the PNN to play a role in the “capture” of the homeodeomain transcription factor orthodenticle homeobox 2 (Otx2) from thalamic inputs to visual cortex (Beurdeley et al., 2012)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Beurdeley et al., 2012
In the citing paper
“Namely, PNNs permit Otx2 capture and transfer into GABAergic interneurons expressing parvalbumin.”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Beurdeley et al., 2012
In the citing paper
“Indeed, the maturation and phenotypic maintenance of PVI require incorporation of a non-cell autonomous homeobox protein, Otx2, through its affinity with PNN (Beurdeley et al., 2012; Miyata et al., 2012).”
From Redox dysregulation, neuroinflammation, and NMDA receptor hypofunction: A “central hub” in schizophrenia pathophysiology? (2016) · cites this paper as Beurdeley et al., 2012
In the citing paper
“PNNs also facilitate the capture and uptake of the transcription factor Otx2, which in turn promotes PVBC maturation as well as further PNN development (100, 173, 912, 1063).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [100]
In the citing paper
“PNNs also facilitate the capture and uptake of the transcription factor Otx2, which in turn promotes PVBC maturation as well as further PNN development (100, 173, 912, 1063).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [100]
In the citing paper
“Similarly, blocking the ability of Otx2 to bind to PNNs results in their degradation and reopens the critical period in adults (100).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [100]
In the citing paper
“In contrast, removing PNNs or reducing Otx2 uptake reopens plasticity in adulthood (Beurdeley et al., 2012; Pizzorusso et al., 2002; Spatazza et al., 2013).”
From Clock Genes Control Cortical Critical Period Timing (2015) · cites this paper as Beurdeley et al., 2012
In the citing paper
“which in turn contributes to closure of critical period plasticity (Beurdeley et al., 2012; Carulli et al., 2010; Pizzorusso et al., 2002).”
From Clock Genes Control Cortical Critical Period Timing (2015) · cites this paper as Beurdeley et al., 2012
In the citing paper
“With PV-cell maturation, perineuronal nets (PNNs) of extracellular matrix molecules condense around their somata”
From Clock Genes Control Cortical Critical Period Timing (2015) · cites this paper as Beurdeley et al., 2012
In the citing paper
“The maturation of PNNs in the developing cortex coincides with the closure of the critical periods of synaptogenesis and circuit refinement (Beurdeley et al., 2012; Ye and Miao, 2013).”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Beurdeley et al., 2012
In the citing paper
“PNNs are thought to limit plasticity and are responsible for the closure of the critical period for ocular dominance in the visual cortex (28).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [28]
In the citing paper
“OTX2 produced in the choroid plexus binds to PNNs in the visual cortex where it facilitates the expression of PNNs (28).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [28]
In the citing paper
“Continual binding of OTX2 to PNNs has been shown to be necessary for synaptic stability in the adult visual cortex and blocking OTX2 uptake into PV+ cells in adults has been demonstrated to reduce PNN expression and reinstate juvenile levels of plasticity (28).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [28]
In the citing paper
“Continual binding of OTX2 to PNNs has been shown to be necessary for synaptic stability in the adult visual cortex and blocking OTX2 uptake into PV+ cells in adults has been demonstrated to reduce PNN expression and reinstate juvenile levels of plasticity (28).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [28]
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Citations
Cites
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323
Self-citationCortical inhibitory neurons and schizophrenia
Lewis, D. A., Hashimoto, T., & Volk, D. W. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1648 · Cited by 2,297
Reactivation of Ocular Dominance Plasticity in the Adult Visual Cortex
Pizzorusso, T., Medini, P., Berardi, N., Chierzi, S., Fawcett, J. W., & Maffei, L. (2002) · Science · doi:10.1126/science.1072699 · Cited by 1,679
Molecular modeling of protein-glycosaminoglycan interactions.
Cardin, A. D., & Weintraub, H. J. R. (1989) · Arteriosclerosis An Official Journal of the American Heart Association Inc · doi:10.1161/01.atv.9.1.21 · Cited by 1,301
Hensch, T. K. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144327 · Cited by 1,300
Self-citationWiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.978 · Cited by 1,291
Experience-Dependent Plasticity of Binocular Responses in the Primary Visual Cortex of the Mouse
Gordon, J. A., & Stryker, M. P. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03274.1996 · Cited by 856
Perineuronal Nets Protect Fear Memories from Erasure
Gogolla, N., Caroni, P., Lüthi, A., & Herry, C. (2009) · Science · doi:10.1126/science.1174146 · Cited by 760
Antennapedia homeobox peptide regulates neural morphogenesis.
Joliot, A., Pernelle, C., Bazin, H., & Prochiantz, A. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.5.1864 · Cited by 653
Self-citationCommon circuit defect of excitatory-inhibitory balance in mouse models of autism
Gogolla, N., LeBlanc, J. J., Quast, K. B., Südhof, T. C., Fagiolini, M., & Hensch, T. K. (2009) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-009-9023-x · Cited by 610
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Items 101–200 of 397
Miyata, S., Nadanaka, S., Igarashi, M., & Kitagawa, H. (2018) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2018.00003 · Cited by 68
Neuroplasticity of the visual cortex: in sickness and in health
Baroncelli, L., & Lunghi, C. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113515 · Cited by 79
Ho, K. H., & Patrizi, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-82800-5 · Cited by 65
Pitts, M. W., Kremer, P. M., Hashimoto, A. C., Torres, D. J., Byrns, C. N., Williams, C. S., & Berry, M. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2724-15.2015 · Cited by 65
Yang, S., Hilton, S., Alves, J. N., Saksida, L. M., Bussey, T., Matthews, R. T., Kitagawa, H., Spillantini, M. G., Kwok, J. C. F., & Fawcett, J. W. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.08.002 · Cited by 61
Tanti, A., Belliveau, C., Nagy, C., Maitra, M., Denux, F., Perlman, K., Chen, F. Y., Mpai, R., Canonne, C., Théberge, S., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01372-y · Cited by 71
Yamada, J., & Jinno, S. (2017) · Journal of Comparative Neurology · doi:10.1002/cne.24132 · Cited by 59
Spatazza, J., Lullo, E. D., Joliot, A., Dupont, E., Moya, K. L., & Prochiantz, A. (2013) · Pharmacological Reviews · doi:10.1124/pr.112.006577 · Cited by 78
Self-citationRupert, D. D., & Shea, S. D. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.886629 · Cited by 58
OTX2 Signals from the Choroid Plexus to Regulate Adult Neurogenesis
Planques, A., Moreira, V. O., Dubreuil, C., Prochiantz, A., & Nardo, A. A. D. (2019) · eNeuro · doi:10.1523/eneuro.0262-18.2019 · Cited by 60
Self-citationIncubation of depression: ECM assembly and parvalbumin interneurons after stress
Spijker, S., Koskinen, M.-K., & Riga, D. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.07.015 · Cited by 55
Diurnal changes in perineuronal nets and parvalbumin neurons in the rat medial prefrontal cortex
Harkness, J. H., Gonzalez, A. E., Bushana, P. N., Jorgensen, E. T., Hegarty, D. M., Nardo, A. A. D., Prochiantz, A., Wisor, J. P., Aicher, S. A., Brown, T. E., et al. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02229-4 · Cited by 55
Self-citationToward Libraries of Biotinylated Chondroitin Sulfate Analogues: From Synthesis to In Vivo Studies
Despras, G., Bernard, C., Perrot, A., Cattiaux, L., Prochiantz, A., Lortat‐Jacob, H., & Mallet, J. (2012) · Chemistry - A European Journal · doi:10.1002/chem.201202173 · Cited by 51
Self-citationThe malleable brain: plasticity of neural circuits and behavior – a review from students to students
Schaefer, N., Rotermund, C., Blumrich, E., Lourenco, M. V., Joshi, P., Hegemann, R. U., Jamwal, S., Ali, N., Romero, E. M. G., Sharma, S., et al. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14107 · Cited by 54
Methylation in OTX2 and related genes, maltreatment, and depression in children
Kaufman, J., Wymbs, N. F., Montalvo‐Ortiz, J. L., Orr, C., Albaugh, M. D., Althoff, R. R., O’Loughlin, K., Holbrook, H. M., Garavan, H., Kearney, C., et al. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0157-y · Cited by 52
Perineuronal Nets: Subtle Structures with Large Implications
Carceller, H., Gramuntell, Y., Klimczak, P., & Nácher, J. (2022) · The Neuroscientist · doi:10.1177/10738584221106346 · Cited by 54
Caught in the Net: Perineuronal Nets and Addiction
Slaker, M. L., Blacktop, J. M., & Sorg, B. A. (2016) · Neural Plasticity · doi:10.1155/2016/7538208 · Cited by 52
Ribic, A., Crair, M. C., & Biederer, T. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.069 · Cited by 51
Regulation of auditory plasticity during critical periods and following hearing loss
Persic, D., Thomas, M. E., Pelekanos, V., Ryugo, D. K., Takesian, A. E., Krumbholz, K., & Pyott, S. J. (2020) · Hearing Research · doi:10.1016/j.heares.2020.107976 · Cited by 51
Cope, E. C., Zych, A. D., Katchur, N. J., Waters, R. C., Laham, B. J., Diethorn, E. J., Park, C. Y., Meara, W. R., & Gould, E. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01174-2 · Cited by 49
Involvement of chondroitin 6-sulfation in temporal lobe epilepsy
Yutsudo, N., & Kitagawa, H. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.07.009 · Cited by 50
Taylor, S. M., Álvarez-Delfín, K., Saade, C. J., Thomas, J. L., Thummel, R., Fadool, J. M., & Hitchcock, P. F. (2015) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-17616 · Cited by 44
The Physiology of Homeoprotein Transduction
Nardo, A. A. D., Fuchs, J., Joshi, R. L., Moya, K. L., & Prochiantz, A. (2018) · Physiological Reviews · doi:10.1152/physrev.00018.2017 · Cited by 52
Self-citationNon-cell Autonomous OTX2 Homeoprotein Regulates Visual Cortex Plasticity Through Gadd45b/g
Apulei, J., Kim, N., Testa, D., Ribot, J., Morizet, D., Bernard, C., Jourdren, L., Blugeon, C., Nardo, A. A. D., & Prochiantz, A. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy108 · Cited by 51
Self-citationPark, A. T., Tooley, U. A., Leonard, J., Boroshok, A. L., McDermott, C. L., Tisdall, M. D., & Mackey, A. P. (2020) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2020.100909 · Cited by 48
Baho, E., Chattopadhyaya, B., Lavertu-Jolin, M., Mazziotti, R. M., Awad, P. N., Chehrazi, P., Groleau, M., Jahannault-Talignani, C., Sanon, N. T., Vaucher, E., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2881-18.2019 · Cited by 44
Cerebellar perineuronal nets in cocaine-induced pavlovian memory: Site matters
Carbo‐Gas, M., Moreno, J. M. M., Guarque‐Chabrera, J., Vazquez-Sanroman, D. B., Gil‐Miravet, I., Carulli, D., Hoebeek, F. E., Zeeuw, C. I. D., Sanchis‐Segura, C., & Miquel, M. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.07.009 · Cited by 44
Brief dark exposure restored ocular dominance plasticity in aging mice and after a cortical stroke
Stodieck, S. K., Greifzu, F., Goetze, B., Schmidt, K.-F., & Löwel, S. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.09.007 · Cited by 43
Nadanaka, S., Miyata, S., Yaqiang, B., Tamura, J.-I., Habuchi, O., & Kitagawa, H. (2020) · Biomolecules · doi:10.3390/biom10111499 · Cited by 43
Stability in the Face of Change: Lifelong Experience-Dependent Plasticity in the Sensory Cortex
Ribic, A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00076 · Cited by 45
Glycosaminoglycans and Glycomimetics in the Central Nervous System
Rowlands, D., Sugahara, K., & Kwok, J. C. F. (2015) · Molecules · doi:10.3390/molecules20033527 · Cited by 44
Chondroitin 4- O -sulfation regulates hippocampal perineuronal nets and social memory
Huang, H., Joffrin, A. M., Zhao, Y., Miller, G. M., Zhang, G. C., Oka, Y., & Hsieh‐Wilson, L. C. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2301312120 · Cited by 43
Treatment of amblyopia in the adult: insights from a new rodent model of visual perceptual learning
Bonaccorsi, J., Berardi, N., & Sale, A. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00082 · Cited by 42
Bernard, C., Vincent, C., Testa, D., Bertini, E., Ribot, J., Nardo, A. A. D., Volovitch, M., & Prochiantz, A. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006035 · Cited by 55
Self-citationSalinas, K. J., Velez, D. X. F., Zeitoun, J. H., Kim, H., & Gandhi, S. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1484-17.2017 · Cited by 41
Inhibition of Semaphorin3A Promotes Ocular Dominance Plasticity in the Adult Rat Visual Cortex
Boggio, E. M., Ehlert, E. M., Lupori, L., Moloney, E. B., De Winter, F., Vander Kooi, C. W., Baroncelli, L., Mecollari, V., Blits, B., Fawcett, J. W., et al. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1499-0 · Cited by 41
Graded Otx2 activities demonstrate dose-sensitive eye and retina phenotypes
Bernard, C., Kim, H.-T., Torero Ibad, R., Lee, E. J., Simonutti, M., Picaud, S., Acampora, D., Simeone, A., Di Nardo, A. A., Prochiantz, A., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddt562 · Cited by 39
Self-citationDzyubenko, E., Manrique‐Castano, D., Kleinschnitz, C., Faissner, A., & Hermann, D. M. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.08.001 · Cited by 40
Bidirectional transfer of homeoprotein EN2 across the plasma membrane requires PIP2
Amblard, I., Dupont, E., Alves, I. D., Miralvès, J., Quéguiner, I., & Joliot, A. (2020) · Journal of Cell Science · doi:10.1242/jcs.244327 · Cited by 35
Alonge, K. M., Logsdon, A. F., Murphree, T. A., Banks, W. A., Keene, C. D., Edgar, J. S., Whittington, D., Schwartz, M. W., & Guttman, M. (2019) · Glycobiology · doi:10.1093/glycob/cwz060 · Cited by 38
Critical aspects of neurodevelopment
Chakraborty, R., Kumar, M., & Clement, J. P. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107415 · Cited by 41
The mechanisms of perineuronal net abnormalities in contributing aging and neurological diseases
Dong, Y., Zhao, K., Qin, X., Du, G., & Gao, L. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102092 · Cited by 39
Perineuronal nets gain prominence for their role in learning, memory, and plasticity
Shen, H. H. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1815273115 · Cited by 39
The potential of memory enhancement through modulation of perineuronal nets
Duncan, J. A., Foster, R., & Kwok, J. C. F. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14672 · Cited by 41
Inhibitory control in neuronal networks relies on the extracellular matrix integrity
Dzyubenko, E., Fleischer, M., Manrique‐Castano, D., Borbor, M., Kleinschnitz, C., Faissner, A., & Hermann, D. M. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03861-3 · Cited by 38
Bitanihirwe, B. K. Y., Mauney, S. A., & Woo, T.-U. W. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.03.1047 · Cited by 40
Neurocan Contributes to Perineuronal Net Development
Schmidt, S., Arendt, T., Morawski, M., & Sonntag, M. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.06.040 · Cited by 36
Santos‐Silva, T., Colodete, D. A. E., Lisboa, J. R., Freitas, I. D. S., Lopes, C. F. B., Hadera, V., Lima, T. S. A., Souza, A. J., & Gomes, F. V. (2024) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13994 · Cited by 39
Subtypes of GABAergic cells in the inferior colliculus
Schofield, B. R., & Beebe, N. L. (2018) · Hearing Research · doi:10.1016/j.heares.2018.10.001 · Cited by 36
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Gibel-Russo, R., Benacom, D., & Nardo, A. A. D. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.875873 · Cited by 37
Mueller-Buehl, C., Reinhard, J., Roll, L., Bader, V., Winklhofer, K. F., & Faissner, A. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.886527 · Cited by 37
MacMullin, P., Hodgson, N., Damar, U., Lee, H. H. C., Hameed, M. Q., Dhamne, S. C., Hyde, D. E., Conley, G. M., Morriss, N. J., Qiu, J., et al. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa157 · Cited by 36
Self-citationWegrzyn, D., Freund, N., Faissner, A., & Juckel, G. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.637549 · Cited by 37
Global Analysis of Intercellular Homeodomain Protein Transfer
Lee, E. J., Kim, N., Park, J. W., Kang, K. H., Kim, W.-I., Sim, N. S., Jeong, C.-S., Blackshaw, S., Vidal, M., Huh, S., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.056 · Cited by 37
A conceptualized model linking matrix metalloproteinase-9 to schizophrenia pathogenesis
Bitanihirwe, B. K. Y., & Woo, T.-U. W. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2019.12.015 · Cited by 35
Regulation of retinal axon growth by secreted Vax1 homeodomain protein
Kim, N., Min, K. W., Kang, K. H., Lee, E. J., Kim, H.-T., Moon, K., Choi, J., Dai, L., Lee, S.-H., & Kim, J. W. (2014) · eLife · doi:10.7554/elife.02671 · Cited by 40
Regulation of the E/I-balance by the neural matrisome
Mueller-Buehl, C., Wegrzyn, D., Bauch, J., & Faissner, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1102334 · Cited by 35
Reinhard, S. M., Rais, M., Afroz, S., Hanania, Y., Pendi, K., Espinoza, K., Rosenthal, R., Binder, D. K., Ethell, I. M., & Razak, K. A. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107042 · Cited by 37
Mascio, G., Notartomaso, S., Martinello, K., Liberatore, F., Bucci, D., Imbriglio, T., Cannella, M., Antenucci, N., Scarselli, P., Lattanzi, R., et al. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1714-21.2022 · Cited by 32
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Donegan, J. J., & Lodge, D. J. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw095 · Cited by 35
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Van’t Spijker, H. M., Rowlands, D., Rossier, J., Haenzi, B., Fawcett, J. W., & Kwok, J. C. F. (2019) · Neural Plasticity · doi:10.1155/2019/6804575 · Cited by 31
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Mitchell, D. E., & Duffy, K. R. (2014) · Ophthalmic and Physiological Optics · doi:10.1111/opo.12122 · Cited by 32
Perineuronal nets and GABAergic cells in the inferior colliculus of guinea pigs
Foster, N. L., Mellott, J. G., & Schofield, B. R. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00053 · Cited by 30
The Role of Perineuronal Nets in Physiology and Disease: Insights from Recent Studies
Auer, S., Schicht, M., Hoffmann, L., Budday, S., Frischknecht, R., Blümcke, I., & Paulsen, F. P. (2025) · Cells · doi:10.3390/cells14050321 · Cited by 32
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Sakai, A., Nakato, R., Ling, Y., Hou, X., Hara, N., Iijima, T., Yanagawa, Y., Kuwano, R., Okuda, S., Shirahige, K., et al. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00307 · Cited by 30
Self-citationTranscriptional maturation of the mouse auditory forebrain
Hackett, T. A., Guo, Y. P., Clause, A. R., Hackett, N., Garbett, K. A., Zhang, P., Polley, D. B., & Mirnics, K. (2015) · BMC Genomics · doi:10.1186/s12864-015-1709-8 · Cited by 30
Emerging Roles of Synapse Organizers in the Regulation of Critical Periods
Ribic, A., & Biederer, T. (2019) · Neural Plasticity · doi:10.1155/2019/1538137 · Cited by 28
Yang, X. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0117 · Cited by 31
MiR‐29 coordinates age‐dependent plasticity brakes in the adult visual cortex
Napoli, D., Lupori, L., Mazziotti, R. M., Sagona, G., Bagnoli, S., Samad, M., Sacramento, E. K., Kirkpartick, J., Putignano, E., Chen, S., et al. (2020) · EMBO Reports · doi:10.15252/embr.202050431 · Cited by 31
The Relative Contributions of Cell-Dependent Cortical Microcircuit Aging to Cognition and Anxiety
Shukla, R., Prévot, T. D., French, L., Isserlin, R., Rocco, B. R., Banasr, M., Bader, G. D., & Sibille, E. L. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.09.019 · Cited by 27
Sugitani, K., Egorova, D., Mizumoto, S., Nishio, S., Yamada, S., Kitagawa, H., Oshima, K., Nadano, D., Matsuda, T., & Miyata, S. (2021) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2020.129804 · Cited by 28
Non-cell-autonomous OTX2 transcription factor regulates anxiety-related behavior in the mouse
Vincent, C., Gilabert‐Juan, J., Gibel-Russo, R., Alvarez‐Fischer, D., Krebs, M., Pen, G. L., Prochiantz, A., & Nardo, A. A. D. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01132-y · Cited by 32
Self-citationJakovljević, A., Tucić, M., Blažíková, M., Korenić, A., Missirlis, Y. F., Stamenković, V., & Anđjus, P. R. (2021) · Cells · doi:10.3390/cells10061345 · Cited by 32
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Sagan, S., Burlina, F., Alves, I. D., Bechara, C., Dupont, E., & Joliot, A. (2013) · Current Pharmaceutical Design · doi:10.2174/1381612811319160002 · Cited by 28
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Perineuronal net, CSPG receptor and their regulation of neural plasticity.
Miao, Q., Ye, Q., & Zhang, X.-H. (2014) · PubMed · Cited by 27
Molecular mechanisms of experience‐dependent maturation in cortical GABA ergic inhibition
Begum, M., & Sng, J. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14103 · Cited by 27
Yamada, J., & Jinno, S. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23712 · Cited by 27
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Corredor, M., Bonet, R., Moure, A., Domingo, C., Bujons, J., Alfonso, I., Pérez, Y., & Messeguer, Á. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.01.033 · Cited by 30
Lau, B. Y. B., Layo-Carris, D. E., Emery, B. A., Everett, M., Kumar, A., Stevenson, P. K., Reynolds, K. G., Cherosky, A., Bowyer, S.-A. H., Roth, S., et al. (2020) · eNeuro · doi:10.1523/eneuro.0500-19.2020 · Cited by 29
Acan downregulation in parvalbumin GABAergic cells reduces spontaneous recovery of fear memories
Lavertu-Jolin, M., Chattopadhyaya, B., Chehrazi, P., Carrier, D., Wünnemann, F., Leclerc, S., Dumouchel, F., Robertson, D. N., Affia, H., Saba, K., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02085-0 · Cited by 27
Mitochondrial Protection by Exogenous Otx2 in Mouse Retinal Neurons
Kim, H.-T., Kim, S. J., Sohn, Y.-I., Paik, S.-S., Caplette, R., Simonutti, M., Moon, K. H., Lee, E. J., Min, K. W., Kim, M. J., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.075 · Cited by 25
Transplantation of GABAergic interneurons for cell-based therapy
Spatazza, J., Mancia, W., & Álvarez-Buylla, A. (2017) · Progress in brain research · doi:10.1016/bs.pbr.2016.11.005 · Cited by 25
Self-citationForostyak, S., Forostyak, O., Kwok, J. C. F., Romanyuk, N., Řehořová, M., Kriška, J., Dayanithi, G., Raha‐Chowdhury, R., Jendelová, P., Anděrová, M., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249593 · Cited by 24
The Role and Modulation of Spinal Perineuronal Nets in the Healthy and Injured Spinal Cord
Sánchez-Ventura, J., Lane, M. A., & Udina, E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.893857 · Cited by 26
Biology-driven material design for ischaemic stroke repair
Phan, N. V., Rathbun, E. M., Ouyang, Y., Carmichael, S. T., & Segura, T. (2023) · Nature Reviews Bioengineering · doi:10.1038/s44222-023-00117-6 · Cited by 26
Igarashi, M., Takeuchi, K., & Sugiyama, S. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.10.001 · Cited by 22
Self-citationMurase, S., Winkowski, D. E., Liu, J., Kanold, P. O., & Quinlan, E. M. (2019) · eLife · doi:10.7554/elife.52503 · Cited by 24
Lee, H. H. C., Pearl, P. L., & Rotenberg, A. (2021) · Journal of Child Neurology · doi:10.1177/0883073821993000 · Cited by 22
Self-citationSexually dimorphic perineuronal net expression in the songbird
Meyer, C., Boroda, E., & Nick, T. A. (2013) · Basal Ganglia · doi:10.1016/j.baga.2013.10.002 · Cited by 22
The Extracellular Matrix in the Nervous System: The Good and the Bad Aspects
Vecino, E., & Kwok, J. C. F. (2016) · InTech eBooks · doi:10.5772/62527 · Cited by 26
O’Connor, A. M., Burton, T. J., Mansuri, H., Hand, G. R., Leamey, C. A., & Sawatari, A. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00090 · Cited by 21
Neuroanatomical Alterations in the CNTNAP2 Mouse Model of Autism Spectrum Disorder
Gandhi, T., Canepa, C. R., Adeyelu, T. T., Adeniyi, P. A., & Lee, C. C. (2023) · Brain Sciences · doi:10.3390/brainsci13060891 · Cited by 22
Adolescent Parvalbumin Expression in the Left Orbitofrontal Cortex Shapes Sociability in Female Mice
Jeon, Y.-S., Jeong, D., Kweon, H., Kim, J., Kim, C. Y., Oh, Y., Lee, Y.-H., Kim, C. H., Kim, S., Jeong, J., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0918-22.2023 · Cited by 23
Kuczynski-Noyau, L., Karmann, S., Alberton, P., Martínez‐Corral, I., Nampoothiri, S. S., Sauvé, F., Lhomme, T., Quarta, C., Apte, S., Bouret, S. G., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50798-9 · Cited by 21
Gene Expression Patterns Underlying the Reinstatement of Plasticity in the Adult Visual System
Tiraboschi, E., Guirado, R., Greco, D., Auvinen, P., Maya‐Vetencourt, J. F., Maffei, L., & Ċastrén, E. (2013) · Neural Plasticity · doi:10.1155/2013/605079 · Cited by 25
Shimbo, M., Suzuki, R., Fuseya, S., Sato, T., Kiyohara, K., Hagiwara, K., Okada, R., Wakui, H., Tsunakawa, Y., Watanabe, H., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0190333 · Cited by 21
Homeoprotein transduction in neurodevelopment and physiopathology
Nardo, A. A. D., Joliot, A., & Prochiantz, A. (2020) · Science Advances · doi:10.1126/sciadv.abc6374 · Cited by 20
Self-citationOrlando, C., & Raineteau, O. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0701-9 · Cited by 22
Metadata
- Authors
- Beurdeley, M., Spatazza, J., Lee, H. H. C., Sugiyama, S., Bernard, C., Di Nardo, A. A., Hensch, T. K., & Prochiantz, A.
- Affiliations
- Collège de France (FR)
- Centre National de la Recherche Scientifique (FR)
- Boston Children's Hospital (US)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2012-07-04
- Volume
- 32
- Issue
- 27
- Pages
- 9429-9437
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3419577
- OpenAlex
- W2040502575
- Cited by
- 398
- References
- 50
- Citations by year
- 2026: 17 · 2025: 25 · 2024: 21 · 2023: 28 · 2022: 22 · 2021: 38 · 2020: 37 · 2019: 38 · 2018: 26 · 2017: 34 · 2016: 22 · 2015: 32 · 2014: 29 · 2013: 26 · 2012: 3
- FWCI
- 9.69
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- other-oa
- Locations
- Journal of Neuroscience (publishedVersion, other-oa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- HAL (submittedVersion, other-oa)
- Funders
- Agence Nationale de la Recherche
- Croucher Foundation
- Ministry of Education, Science and Technology
- Centre National de la Recherche Scientifique
- National Institutes of Health (DP1OD003699)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- Otx2, perineuronal nets, critical period, visual cortex plasticity, parvalbumin interneurons, glycosaminoglycan binding, chondroitin sulfate, chondroitinase ABC, amblyopia, binocular vision, homeodomain transcription factor
- MeSH terms
- Age Factors, Animals, Extracellular Matrix, Interneurons, Male, Mice, Inbred C57BL, Neuronal Plasticity, Protein Binding, Visual Cortex, Mice, Otx Transcription Factors, GABAergic Neurons
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